DISCLAIMER
The information and materials accessed through or made available for use on any of our Sites, including, any information about diseases, conditions, treatments, or medicines, are for informational purposes only. The Content is not intended to be and is not a substitute for professional medical advice, diagnosis, or treatment, and your participation on our Sites does not create a healthcare professional-patient relationship. You should consult a doctor or other qualified health care professional regarding any questions you have about your health or before making any decisions related to your health or wellness. Call your doctor or 911 immediately if you think you may have a medical emergency.compose your message
message sent
email sent successfully
Trusted Resources: Community Center
Online groups, photo galleries and blogs
Today’s Faces of Sickle Cell Disease: Carolyn Rowley, PhD
Carolyn Rowley is a psychologist, patient advocate, founder and executive director of Cayenne Wellness Center and Children’s Foundation. From a young age, Rowley always had a strong faith and dreamed of one day working as a missionary to improve people’s lives. In a sense, she has fulfilled that dream by embarking on what she considers a divine mission as an advocate for those living with sickle cell disease in California.
As founder and executive director of Cayenne Wellness Center and Children’s Foundation, Rowley has spent nearly 20 years working to reduce the barriers and discrimination faced by individuals with sickle cell disease while increasing awareness among patients, providers, and the public. But she’s not just an advocate; Rowley also is a patient. She experiences the very struggles of those who live daily with the painful disease and yet is determined to create a brighter, more equitable future.
Related Content
-
Community CenterSickle Cell Disease in the Emergency Department: Confronting Barriers to Care“You’re too pretty to have a disease...
-
Community CenterSending a Child With Sickle Cell Disease off to CollegeSickle cell disease afflicts about 100,0...
-
education & researchThe psychosocial impact of leg ulcers in patients with sickle cell disease: I don’t want them to know my littl...BACKGROUND: Sickle cell disease (SCD) i...
-
videos & visualsImproving Quality of Life Through Sickle Cell Research: Marsha J. Treadwell, MDhttps://www.youtube.com/watch?v=DA51AAUH...
-
news & eventsSickle Cell Disease Association of America, Inc. Names New CEO & PresidentThe Sickle Cell Disease Association of A...
-
people & placesDiana Wells RN, MSW, MPHDiana Wells serves as a clinical social ...
-
news & eventsRare Disease Day Symposium at the Quinnipiac Frank H. Netter MD School of MedicineSince 2015, the Frank H. Netter MD Schoo...
send a message
To improve your experience on this site, we use cookies. This includes cookies essential for the basic functioning of our website, cookies for analytics purposes, and cookies enabling us to personalize site content. By clicking on 'Accept' or any content on this site, you agree that cookies can be placed. You may adjust your browser's cookie settings to suit your preferences. More Information
The cookie settings on this website are set to "allow cookies" to give you the best browsing experience possible. If you continue to use this website without changing your cookie settings or you click "Accept" below then you are consenting to this.